US3692757A

US3692757A - Thermosetting acrylics containing oxazoline groups

Info

Publication number: US3692757A
Application number: US89116A
Authority: US
Inventors: Rostyslaw Dowbenko
Original assignee: PPG Industries Inc
Current assignee: PPG Industries Inc
Priority date: 1967-09-06
Filing date: 1970-11-12
Publication date: 1972-09-19
Anticipated expiration: 1989-09-19

Abstract

Novel polymerizable unsaturated oxazoline compounds are obtained by dehydrating a hydroxyalkyl-substituted amino-ethanol and esterifying or transesterifying the resulting alcohol with an ethylenically unsaturated monocarboxylic acid, an ester of such an acid, or an ethylenically unsaturated monocarboxylic acid halide. Preferred embodiments include 2,4-dialkyl-2-oxazoline-4alkyl acrylates and methacrylates. Polymers of such compounds, and particularly their inter-polymers with other ethylenic monomers provide thermosetting film-forming compositions, useful as protective coatings and adhesives.

Description

United States Patent Dowbenko n51 3,692',757 [451 Sept. 19, 1972 THERMOSETTING ACRYLICS CONTAINING OXAZOLINE GROUPS [72] Inventor: Rostyslaw Dowhenko, Gisbornia, Pa.

[73] Assignee: PPG Industries, Inc., Pittsburgh, Pa.

[22] Filed: Nov. 12, 1970 [21] App1.No.: 89,116

Related US. Application Data [62] Division of Ser. No. 665,745, Sept. 6,. 1967,

Pat. No. 3,609,161.

[58] Field of Search ..260/80.72, 86.1 N, 89.1

[56] References Cited UNITED STATES PATENTS 3,208,981 '9/1965 Mirandaetal... 2601785 3,380,975 4/1968 Purcell ..260l80.72

Primary Examiner-Joseph L. Schofer Assistant Examiner-Stanford M. Levin Attorney-Chisholm & Spencer [57] ABSTRACT Novel polymerizable unsaturated .oxazoline compounds are obtained by dehydrating a hydroxyalkylsubstituted amino-ethanol and esterifying or transesterifying the resulting alcohol with an ethylenlcally unsaturated monocarboxylic acid, an ester of such an acid, or an ethylenically unsaturated monocarboxylic acid halide. Preferred embodiments include 2,4-dialkyl-2-oxazoline-4-alkyl acrylates and 1 methacrylates. Polymers of such compounds, and particularly their inter-polymers with other ethylenic monomers provide thermosetting film-forming compositions, useful as protective coatings and adhesives.

6 Claims, No Drawings THERMOSETTING ACRYLICS CONTAINING OXAZOLINE GROUPS This application is a division of Application Ser. No. 665,745, filed Sept. 6, 1967, now U. S. Pat. No. 3,609,161, issued Sept. 28, 1971.

Vinyl interpolymers are useful in coatings because of their excellent durability and weatherability, solvent resistance, and adhesion. However, it is difficult to obtain vinyl polymers having the combination of properties necessary to provide coatings of over-all utility for many applications. For instance, cured coatings of sufficient adhesion and hardness tend to have insufficient flexibility for many desired uses, and compositions having suitable application characteristics often are deficient in coating properties. Thus, polymers which can provide improvement in several properties without sacrificing others are of continuing and increasing interest.

The present invention provides new thermosetting resinous compositions which provide coatings having an excellent over-all combination of properties. These compositions comprise polymers of novel monoesters of (l) a polymerizable ethylenically unsaturated monocarboxylic acid, and (2) a substituted oxazoline alcohol. Polymers and interpolymers of such monoesters with vinyl monomers have excellent crosslinking characteristics, and form tough, hard, adherent films with improved properties such as weatherability and solvent resistance.

Although the monoesters are described generally as being a monoester of a monocarboxylic acid and substituted oxazoline alcohol, the novel monoester of this invention can be made by reacting the substituted-oxazoline alcohol with not only the monocarboxylic acid, but also the esters or the acid halides thereof. The product of all of these reactions will be the monoester so generically described.

The new monoesters of the polymerizable ethylenically unsaturated monocarboxylic acid and a sub stituted-oxazoline alcohol are obtained by first dehydrating a hydroxy-substituted aminoethanol with a carboxylic acid and esterifying or transesterifying the resulting product with a polymerizable ethylenically unsaturated monocarboxylic acid or an ester thereof, or an ethylenically unsaturated monocarboxylic acid halide.

The dehydration reaction between the carboxylic acid and the hydroxy-substituted aminoethanol proceeds in accordance with the following equation:

wherein R, is selected from the group consisting of alkyl groups, hydrogen, and aryl groups; R is selected from the group consisting of alkylene and alkyl aryl groups; and R is selected from the group consisting of alkyl groups, aryl groups, and alkyl aryl groups. The product is a substituted-oxazoline alcohol.

The starting material can be any hydroxyalkyl-substituted aminoethanol, although the preferred starting compound is a l,3'dihydroxy-2-aminopropane. The length of the alkyl or aryl group of R and the alkylene or alkyl aryl group of R is immaterial, but the preferred compounds contain alkyl groups with one to ten carbon atoms such as methyl, ethyl, isopropyl, hexyl, octyl and decyl groups, or alkyl aryl (alkaryl) groups wherein the alkyl portion contains one to ten carbon atoms such as benzyl, phenylethyl, phenyloctyl, and phenyldecyl groups, and alkylene groups with one to ten carbon atoms such as methylene, ethylene, isopropylene, hexylene, and octylene groups. Some examples of hydroxy-substituted aminoethanols are 2- methyl-2-amino-l ,3-dihydroxy-propane, 2-amino-l ,3-

dihydroxy-Z-methylpentane, 2-amino-l ,3-dihydroxy-2- ethyl-4-methylpentane, 2-amino-l ,4-dihydroxy-2- ethyl-3-methylbutane, 2-amino-l ,5-dihydroxy-2- isopropylpentane, l-hydroxy-2-amino-2-[4-(2-hydroxyethyl) phenyl] propane, l-hydroxy-2-amino-2-[4- (hydroxymethyl) phenyl] butane, and others following the general description above. Compounds containing more than two primary hydroxy groups, such as amino trimethylol methane, are not included in the class of starting materials described.

The acid used to dehydrate the hydroxy-substituted aminoethanol can be any carboxylic acid following the description given above. Examples are acetic acid, propionic acid, formic acid, fatty acids, phenylpropionic acid, benzoic acid, and other aromatic acids, etc. In a preferred embodiment, acetic acid is utilized. The reaction conditions used to produce the substituted-oxazoline alcohol are not critical. It is only necessary that enough acid be present to dehydrate the hydroxyalkyl substituted aminoethanol. No solvent is necessary, and the temperature of the reaction may be varied over a wide range, although it is preferred to carry out the reaction at temperatures of about 100 C. to 250 C. to increase the speed of reaction.

The product of the dehydration reaction is a sub stituted-oxazoline alcohol of the formula:

wherein R R and R are as above. This substitutedoxazoline alcohol is then esterified or transesterified with a polymerizable ethylenically unsaturated monocarboxylic acid, an ester thereof, or an ethylenically unsaturated monocarboxylic acid halide to form the new compounds of this invention.

The esterification or transesterification can be accomplished by reacting the substituted-oxazoline -alcohol with any polymerizable ethylenically unsaturated monocarboxylic acid or ester, or ethylenically unsaturated monocarboxylic acid halide. For example, acrylic acid, methacrylic acid, crotonic acid, and alkyl esters of such acids including alkyl methacrylates, such as methyl methacrylate, ethyl methacrylate, isopropyl methacrylate, and hexyl methacrylate, and alkyl acrylates, such as methyl acrylate, isopropyl acrylate, ethyl acrylate, and octyl acrylate, and alkyl crotonates, such as methyl crotonate, ethyl crotonate, and octyl crotonate, can be employed, as can acrylyl halides, methacrylyl halides, and crotonyl halides, such as acrylyl chloride, methacrylyl bromide, crotonyl fluoride, and others. The preferred reactants are methyl methacrylate, methacrylyl chloride, acrylic acid, and methacrylic acid.

The esterification or transesterification reaction conditions are not critical. The reaction can be carried out at room temperature; however, it is preferred to use temperatures from about 90 C. to 125 C. to increase the speed of reaction. The ratio of reactants, also, is not critical.

The esteriflcation or transesteriflcation may be aided by the use of a catalyst, such as tetraisopropyl titanate or an alkali metal hydroxide. Examples of catalysts that may be used include: potassium hydroxide, magnesium hydroxide, methyl titanates, and tetrabutyl titanate. The materials can be added to the reaction in any order but it is preferred thatthe addition of the substitutedoxazoline alcohol to the solvent be carried out first if a solvent such as benzene or trichloromethane is used, and the solution allowed to cool before adding the carboxylic acid, its ester, or halide, and refluxing. If such a catalyst is present, it is ordinarily employed in an amount between about 0.1 percent and percent by weight of the starting substituted-oxazoline alcohol. The resulting product of the reaction is the novel monoester.

The above novel monoesters are particularly useful in polymers for various purposes. They are addition polymerized by a free-radical initiated reaction to provide a thermosetting polymer. The polymer can be cross-linked, for example, by heating by itself or in the presence of a dicarboxylic acid.

While the homopolymers described above have excellent properties for some purposes, the preferred polymers of the invention contain at least one other unsaturated monomer interpolymerized with the monoester to form a thermosetting resinous interpolymer.

Any polymerizable monomeric compound containing at least one group may be polymerized with the novel monoester. Examples of such monomers include the following:

Monoolefinic and diolefinic hydrocarbons, such as styrene, alpha-alkylstyrene, vinyltoluene, isobutylene, ethylene, propylene, butylene, isoprene, and the like; Halogenated monoolefinic and diolefinic hydrocarbons, such as alpha-chlorostyrene, 2,5- dibromostyrene, 2-chloro-propene, l, l dichloroethylene, chlorobutadiene, and other halogenated dioleflnic compounds;

Esters of organic and inorganic acids, such as vinyl propionate, vinyl methoxybenzoate, methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, hexyl methacrylate, octyl methacrylate, decyl methacrylate, lauryl methacrylate, Z-hydroxyethyl methacrylate, methyl crotonate, ethyl tiglate, methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, butyl acrylate, hexyl acrylate, 2-ethylhexyl acrylate, decyl acrylate, dodecyl acrylate, Z-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, isopropenyl acetate, vinyl chloroacetate, allyl chloride, allyl acetate, beta-ethylallyl chloride,

methyl alpha-chloro-acrylate. and dimethyl maleate; Organic nitriles, such as acrylonitrile methacrylonitrile, ethacrylonitrile, and the like; Acid monomers, such as acrylic acid, methacrylic acid, crotonic acid, 3-butenoic acid, tiglic acid, angelic acid, methyl hydrogen maleate, butyl hydrogen fumarate, and the like. It is to be understood that the above polymerizable olefinic monomers are representative only and do not include all of the containing monomers which may be employed.

An important advantage of the monoesters of the invention is that they form useful interpolymers as described. Diesters of this general class begin to gel at once in the presence of a vinylic monomer, such as styrene, so that interpolymerization cannot be effected. Hence, such diesters are not useful in the present invention.

In carrying out the polymerization reaction, a freeradical initiating type catalyst, particularly a peroxygen or an azo compound, is ordinarily utilized. The most useful compound found is azo bis(isobutyronitrile). Other useful catalysts for this purpose include acetyl peroxide, benzoyl peroxide, hydroxyheptyl peroxide, methyl ethyl ketone peroxide, 2,4-dichlorobenzoyl peroxide, cumene hydroperoxide, t-butyl hydroperoxide, methyl amyl ketone peroxide, p-chlorobenzoyl peroxide, peracetic acid, t-butyl permaleic acid, t-butyl peracetate, isopropyl peroxy dicarbonate, and the like. In some polymerization reactions, mixtures of the above peroxygen compounds are used to secure desired conversions.

The quantity of catalyst employed can vary considerably; however, in most instances, it is most desirable to utilize from about 0.1 percent to 3 percent. lf high viscosities are desired, a low initial level of catalyst, followed by the necessary additions to get percent conversion, is preferably employed. For low viscosity inter-polymers, the bulk of the catalyst is added initially and later additions used only to secure desired conversions. Larger amounts of catalysts added initially give lower viscosities.

Since it is desirable that the interpolymers of the monoesters of the oxazoline compounds with other ethylenically unsaturated monomers be relatively low in molecular weight so that they can be dissolved at high solids and low viscosity, a chain-modifying agent, or chain terminaton'may be added to the polymerization mixture. The mercaptans, such as dodecyl mercaptan, tertiary dodecyl mercaptan, octyl mercaptan, hexyl mercaptan, and the like, are conventionally used for this purpose, although other chain-modifying agents such as cyclopentadiene, and the like can also be used to secure low molecular weights.

The polymerization is best carried out by admixing the monoester of the oxazoline and the other monomer or monomers, the catalysts, and the chain-modifying agent, if any, in a solvent, and refluxing the resulting solution for a time sufflcient to obtain the desired conversion. Ordinarily, the polymerization will be complete in about l to 16 hours.

1 ing theforrnula:

Polymers of the above-described monoesters of the polymerizable ethylenically unsaturated monocarboxylic acid and substituted-oxazoline alcohol are filmforming and can be used as protective coatings, and for similar purposes in which such characteristics are desired. Both homopolymers of these esters and interpolymers with other copolymerizable ethylenically unsaturated monomers are useful as protective coatings. The polymers dry very rapidly to produce flexible films which have excellent mar resistance and other desirable properties. i l

Both the homopolymer and the interpolymers described above also have desirable adhesive qualities which make them useful as bonding agents and adhesaves.

The polymers can be coated onto many substrates, such as metal, wood, glass, etc., to protect the surface and also are useful as films in laminates.

The polymers are easily cured by drying andbaking at a low temperature for a short period. of time to form a glossy solvent-resistant film. The polymers are generally cured by heating at temperatures of from 325 F. to 375 F. for about 7% hour. The curing temperatures of the interpolymer may be lowered by adding a small amount of curing catalyst, such as mono and dibutyl phosphate.

Pigments, such as titanium dioxide, carbon black,- and the like, may be added to the coating composition to form any desired color. Other ingredients normally found in coating compositions, such as germicides, fillers, driers, silicones, and the like, may be added.

The following examples illustrate in detail the preparation of the alcohol-modified oxazoline, the new monoester, and interpolymers of the monoesters with other monomers. The examples are not intended to limit the invention, however, for there are numerous possible variations and modifications. All parts and percentages are by weight and are based non-volatile d solids content, unless otherwise indicated.

EXAMPLE 1 This example illustrates the preparation of a'novel monoester by first dehydrating the hydroxyalkyl-substituted aminoethanol with acid and esterifying the substituted-oxazoline alcohol product with acrylic acid to form 2,4-dimethyl-2-oxazoline-4-methy1 acrylate.

The substituted-oxazoline alcohol was prepared by adding 68 parts of acetic acid to 105.1 parts of 2- methyl-2-amino-1,3-propanediol and refluxing the mixture for four hours at temperatures of from 158C. to 203 C., while removing 40 parts of evolved water. The resulting product was 168.4 parts of a compound hav- The 2,4-dimethyl-4-hydroxymethyl-2-oxazoline prepared above was esterified with acrylic acid by mixing 25.8 parts of the 2,4-dimethyl-4-hydroxymethy1-2- oxazoline with 17.6 parts of benzene, 0.1 part of phenothiazine, and 28.8 parts of acrylic acid. An exothermic reaction took place and after the temperature stabilized, 0.1 1 part of sulfuric acid was added and the mixture was stirred and heated to reflux. After 1% hours, at a temperature of 93 C., another 0.1 1 part of sulfuric acid was added and after two more hours, another 2.2 parts of sulfuric acid were added. The reaction conditions were maintained for 13% hours. The product obtained was 2,4-dimethyl-2-oxazoline-4- methylacrylate.

EXAMPLE 11 A monoester was prepared by the esterification of 2,4-dimethyl-4 hydroxymethy1-2-oxazoline (prepared which had a boiling point range of 54 to 60 C., mm. Hg. and a refractive index of N 1.4502.

EXAMPLE 111 A monoester was prepared by the transesterification of 2,4-dimethyl-4-hydroxymethy1-2-oxazo1ine with methyl methacrylate by the following method:

38.3 parts of 2,4-dimethy1-4-hydroxymethy1-2-oxazoline, and 59.4 parts of methyl methacrylate were added to 1.5 parts of hydroquinone and 0.8 part of tet raisopropyl titanate. These materials were stirred and heated to reflux and the reaction continued for 14 hours at 108 C. The mixture was then cooled, washed with water, and dried over sodium sulfate. The sodium sulfate was filtered off, 0.5 part of hydroquinone was added, and the ether removed. The residue was distilled on a vacuum pump. The product was identical to that obtained in Example 11.

EXAMPLE IV A monoester was prepared by the transesterification of 2.4-dimethyl-4-hydroxymethyl-2-oxazoline with methacrylyl chloride by the following methodz A l-liter flask was charged with 51.7 parts of 2,4- dimethyl-3-hydroxymethyl-2-oxazoline in parts of trichloromethane, to which 45.5 parts of triethylamine were added. To this solution, 41.3 parts of methacrylyl chloride were added dropwise at a steady rate at 25 C. An additional 150 parts of trichloromethane were added and the mixture stirred for three hours. The product was the same as those obtained in Examples 11 and 111.

EXAMPLE V This example illustrates the homopolymerization of the monoester of a polymerizable, ethylenically unsaturated monocarboxylic acid and a substituted-oxazoline saturated monomers. The interpolymer'was alcohol. The monoester used was 2.4-dimethyl-2-oxazoline-4-methyl methacrylate, prepared as in Examples ll, Ill, and IV. The homopolymer was prepared using the method set forth below:

Twenty parts of 2,4-dimethyl-2-oxazoline-4-methyl 5 methacrylate, 70 parts of benzene, and 0.3 part of azo bis(isobutyronitrile) were charged to a reaction vessel and the contents stirred and heated to reflux. After stirring for four hours at 8l C., an additional 10 parts of benzene and 0.2 part of azo bis(isobutyronitrile) were added. The reaction was .run at 81 C. for a total of seven hours. The product had a solids content of 20.1 percent and a viscosity of A. The product was drawn down on a steel panel and baked at 350 F. for 30 minutes. The coating was found to be hard, adherent, but somewhat brittle and had good gloss characteristics and was insoluble in xylene.

- EXAMPLE V] rated monocarboxylic acid and a substituted-oxazoline alcohol with other copolymerizable ethylenically unusing the method set forth below: a

A mixture of 40 parts of xylene and 10 parts of butanol were stirred and heated to 90 C. Ten parts of 2,4- dimethyl-Z-oxazoline-4-methyl methacrylate, 33.3

parts of hydroxyethyl methacrylate, 35.0 parts of 30 dried for A hour, and then baked at 325 F. for A hour. The coating obtained has excellent properties, including excellent adhesion and flexibility. It was solvent re- 4 This product was drawn down on a metal panel, flash prepared 2 and 0.1 part of t-dodecyl mercaptan. An additional 0.2 part of azo bis(isobutyronitrile) was then added. Heating and stirring at 88 to 90 C. was continued for a total of 8 hours. The Gardner-Holdt viscosity of the resulting product was found to be Y-Z, and the solids content was 45.0 percent.

The above composition was drawn down on a metal panel to, test for brittleness, susceptibility to xylene rub test, and mar resistance. The coated panel was baked at 325 F. for v. hour. The coating was found to have fairly good mar resistance, was very flexible, and was only slightly affected by the xylene rub test.

EXAMPLE vm Parts by Weight 2.4-Dimethyl-2-oxuoline- 4-methyl methlcrylate Methyl melhacrylltc 50 Z-Ethylhexyl acrylate 35 Acrylic acld 5 I A vessel was charged with 75 parts of xylene and '25 parts of butanol stirred and heated to 88 to 90C. A mixture of 100 parts of the above ingredients with 0.8 part of azo bis(isobutyronitrile) and 0.1 part of tdodecyl mercaptan was added dropwise. An additional 0.2 part of azo bis(isobutyronitrile) was added, and the heating at 90 C. was continued for a total of eight hours. The resulting interpolymer had a Gardner-Holdt viscosity of X-Y, and the solids content was 48.5 per cent.

The interpolymer was drawn downon a metal panel for testing. The coated panel was flash dried for /5 hour and baked at 325 F. for A hour. The product was 0 similar to that formed in Example Vll.

sistant, as shown by the xylene rub test, where the coat- 5 ing was' rubbed with a cloth saturated with xylene times. Since no appreciable surface change was discemable, the film was determined to be solvent resistant and fully cured.

EXAMPLE Vll An interpolymer was prepared from a mixture of the following materials:

A vessel was charged with parts of xylene and 25 parts of butanol, stirred and heated to C. The above ingredients were added dropwise over a period of 3% hours, along with 0.8 part of azo bis(isobutyronitrile) It is seen that the choice of solvents used is not critical for the interpolymerization. The interpolymer may contain any where from 0 to 99 percent by weight of the new monoester but preferably contains from 1 to 50 percent by weight for these thermosetting systems. Optimum results are obtained by using from 5 to 20 percent by weight of the new monoester.

While there are above described a number of specific embodiments of the present invention, it is obviously possible to produce other embodiments and various equivalent modifications thereof without departing from the spirit of the invention or the scope of the appended claims.

lclaim:

1. A thermosetting ungelled resinous composition comprising a crosslinkable, film-forming polymer of monomers consisting essentially of:

l. a monoester of (a) a polymerizable ethylenically unsaturated monocarboxylic acid; and (b) an alcohol having the formula:

R1 oli e-R201;

0 may 9 wherein R, is selected from the group consisting of hydrogen, alkyl groups containing from about one to about carbon atoms, and aryl groups containing from about one to about 10 carbon atoms, R is selected from the group consisting of alkylene groups containing from about one to about 10 carbon atoms and alkyl aryl groups containing from about one to about 10 carbon atoms, and R is selected from the group consisting of alkyl groups, aryl groups and alkyl aryl groups containing from about one to about 10 carbon atoms, with 2. from 0 to about 99 percent by weight of at least one other copolymerizable ethylenically-unsaturated monomer.

2. The thermosetting ungelled resinous composition monoester comprises from 5 to 20 percent by weight of the interpolymer.

Claims

2. from 0 to about 99 percent by weight of at least one other copolymerizable ethylenically-unsaturated monomer.
2. The thermosetting ungelled resinous composition of Claim 1 wherein the monoester is 2,4-dialkyl-2-oxazoline-4-alkyl methacrylate.
3. The composition of claim 1 wherein the mono-ester is 2,4-dialkyl-2-oxazoline-4-alkyl acrylate.
4. The thermosetting resin of claim 1 wherein the monoester comprises from 1 to 50 percent by weight of the interpolymer.
5. The thermosetting resin of claim 4 wherein one of the other copolymerizable ethylenically unsaturated monomers is methyl methacrylate.
6. The thermosetting resin of claim 1 wherein the monoester comprises from 5 to 20 percent by weight of the interpolymer.